US3313720A - Apparatus for measuring dissolved oxygen in water - Google Patents

Apparatus for measuring dissolved oxygen in water Download PDF

Info

Publication number
US3313720A
US3313720A US274219A US27421963A US3313720A US 3313720 A US3313720 A US 3313720A US 274219 A US274219 A US 274219A US 27421963 A US27421963 A US 27421963A US 3313720 A US3313720 A US 3313720A
Authority
US
United States
Prior art keywords
electrodes
liquid
oxygen
electrode
dissolved oxygen
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US274219A
Inventor
Robinson Richard Hoe
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Labconco Corp
Original Assignee
Labconco Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Labconco Corp filed Critical Labconco Corp
Priority to US274219A priority Critical patent/US3313720A/en
Application granted granted Critical
Publication of US3313720A publication Critical patent/US3313720A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/403Cells and electrode assemblies
    • G01N27/404Cells with anode, cathode and cell electrolyte on the same side of a permeable membrane which separates them from the sample fluid, e.g. Clark-type oxygen sensors

Definitions

  • This invention relates to apparatus for determining the dissolved oxygen content of a liquid and particularly to a direct reading instrument capable of indicating the amount of dissolved oxygen in the liquid by the simple expedient of the operator immersing a probe in the liquid and visually observing the reading on a dissolved oxygen indicator.
  • the amount of dissolved oxygen in a liquid such as water has heretofore been a relatively difiicult analytical operation because of the small amount of oxygen which is actually present in the water and the complicated tests which must be performed in order to accurately determine the presence and amount of the oxygen which is dissolved in the liquid. In most instances, the amount of dissolved oxygen in the liquid will not exceed about ten parts per million and, therefore, requiring very sensitive instruments operated by relatively skilled technicians. Furthermore, it has not heretofore been possible to maintain an accurate surveillance on the amount of dissolved oxygen in a body of water and permitting utilization of the analytical instrument as a device for varying the amount of air or oxygen which is supplied to the water to maintain the dissolved oxygen at a predetermined level.
  • the primary object of the present invention to provide apparatus for measuring dissolved oxygen in a liquid such as water, which requires no laboratory procedures, provides an immediate visual indication of the amount of oxygen in a body of liquid, and which is completely portable for use at any desired location without outside current sources or accessory instruments.
  • a particularly important object of the invention is to provide apparatus as described above, which is utilizable under varying conditions and with the dissolved oxygen readings being accurate within reasonable tolerances, regardless of normal temperature variations in the liquid being measured and the rate of flow thereof relative to the test apparatus,
  • a still further important aim of the invention is to provide apparatus for measuring dissolved oxygen in water wherein the probe is made up of electrodes of thallium, lead and aluminum respectively, operably coupled to a current measuring device so that the amount of oxygen in a liquid in which the probe is immersed, may be readily determined by virtue of reaction of the thallium with the oxygen, thereby producing a measurable current between the electrodes.
  • another significant object of the invention is to provide apparatus as referred to :above, wherein the aluminum electrode is connected to one terminal of the current measuring device, while the thallium and lead electrodes are connected in parallel relationship to the other terminal so that currents of opposite direction are produced between the electrodes to thereby provide compensation for temperature variations in the liquid being tested.
  • Patented Apr. H, 1957 Another very important object of the invention is to provide apparatus employing an electrode probe of thallium, lead and aluminum electrodes operably coupled to a measuring device wherein an ion permeable membrane is provided around each of the electrodes to prevent variations in the flow rates of the liquid being tested atfecting the readings of the current measuring device.
  • Another object of the invention is to provide apparatus capable of measuring the dissolved oxygen content in a flowing liquid which is particularly useful for determining the amount of oxygen in sewage within a sewage treatment facility 50 that the apparatus may be coupled through servo-mechanism or the like to structure for delivering controlled amounts of air or oxygen to the body of sewage in response to variations in the oxygen content sensed by the test apparatus.
  • FIG. 1 is an elevational view of portable test apparatus for measuring the amount of dissolved oxygen in a liquid and constructed in accordance with the preferred Concepts of the present invention, with the probe and container thereof being shown to one side of the instrument case for clarity of illustration;
  • FIG. 2 is a plan view of the apparatus illustrated in FIG. 1 and showing the probe and container therefor in normal disposition on the rear face of the instrument case;
  • FIG. 3 is a schematic representation of the probe and operating circuit therefor provided within the test instrument case.
  • FIG. 4 is a greatly enlarged horizontal cross-sectional view taken substantially on line 4-4 of FIG. 1.
  • Apparatus capable of measuring dissolved oxygen in water is broadly designated It in the drawing, and includes a generally rectangular instrument case 12 mounting a visually observable microammeter 14 on the front face panel 16 thereof so that the operator may readily observe the location of needle 18 with reference to the linear scale 2t).
  • the front face panel 16 of case 12 also mounts a double pole double throw toggle switch 22, a selectively adjustable potentiometer control 24, and a pair of terminals 26 and 28 identified with appropriate positive and negative indicia on panel 16.
  • the upper opening defining extremity of container 34 is internally threaded to complementally receive the external threads of a mounting block 38 which serves as means for mounting elongated, generally cylindrical electrodes 40, 42 and 44 respectively.
  • Electrode 40 is preferably of lead, electrode 42 of aluminum and electrode 44 of thallium.
  • the upper extremities of the electrodes are embedded in block 38 in disposition with the longitudinal axes thereof being in generally parallel relationship with the outer surfaces of the same in equidistant relationship and thereby located at the apices of an imaginary equilateral triangle.
  • the electrodes are also of substantially equal length, as is apparent from FIGS. 1 and 3.
  • a membrane 46 of an ion permeable material is provided around each of the electrodes 40, 42 and 44 in completely encasing relationship thereto with the membrane preferably being of cellulose acetate or cellulose nitrate.
  • the membrane should be of propperties and thickness permitting inorganic ions to pass therethrough but precluding passage of organic molecules and other particles of similar size or larger therethrough.
  • the thallium electrode 44 is connected to the switch arm 48 of selector switch 22 by line while the coil 52 of potentiometer 54 is interposed in a line 56 leading from lead electrode 40 to line 5-0.
  • Line 53 serves to join aluminum electrode 42 directly to line 56.
  • the movable contact 69 of potentiometer 54 is coupled to the positive terminal 62 of microammeter 14 by line 64 while the negative terminal 66 of microarnmeter 14 is joined to switch arm 63 of selector switch 22 by line 74 ⁇ .
  • a load resistor 72 is provided in line 74 between contacts 76 and 78 of switch 22 while line 86 connects terminal 26 to contact 82 of switch 22 and line 84 couples contact 86 of switch 22 to terminal 28.
  • switch arms 43 and 68 are suitably ganged.
  • the conductor lines 56 and 58 extending from case 12 to mounting block 33, are suitably encased in an insulating sheath 83 which is of sufficient length to be immersed in a liquid at a substantial distance from case 12.
  • suitable brackets 90 are provided on surface 32 of case 12 in outwardly extending relationship therefrom, serving as means for storing sheath 88 and the conductors therein when wound around the brackets, as illustrated in FIG. 2.
  • Handle 92 on the top of case 12 facilitates manual transportation of apparatus 10.
  • the container 34 is removed from mounting block 38 and the probe, defined by electrodes 40, 42 and 44 is immersed in the liquid to be tested for dissolved oxygen content.
  • the toggle switch 22 is placed in disposition normally designated as Indicate whereby the switch arms 48 and 68 will be in the disposition thereof illustrated in FIG. 3, placing the load resistor 72 in circuit with the ammeter 14. If the liquid to be measured comprises a flowing stream, it is only necessary that the probe be held in the liquid so that a direct reading may be observed on the dial of meter 14. However, if the water is still, since some water movement or flow is required for accurate determination of the amount of oxygen in the liquid, the probe should be moved back and forth while reading the disposition of needle 18 with respect to the indicia of scale 2t).
  • the liquid containing dissolved oxygen must have approximately four hundred parts per million of dissolved solids in the liquid .in order to give a correct reading on meter 14.
  • Dissolved solids in the context used herein means primarily those materials which will ionize and thus includes inorganic salts although certain types of organic materials would also fall into this catergory.
  • the reading of needle 18 on scale 20 gives a direct indication of the amount of oxygen in the liquid being tested.
  • Empirical studies have shown that the amount of current measured by meter 14 is linearly related to the amount of oxygen in the liquid.
  • apparatus is especially useful for measuring dissolved oxygen in water that contains at least four hundred parts per million of dissolved solids, it has been determined that the most important utility of the present structure is concerned with measurement of the amount of oxygen in sewage within the digestion basin of a sewage treatment facility. It is well known that the amount of oxygen present in the digestion basin of a sewage treatment plant is an extremely important parameter that must be maintained at a predetermined value or above in order to obtain most efficient treatment of the raw sewage. For this reason, it is desirable to have an accurate method available of determining the :amount of oxygen in the sewage in the digestion basin and with such information preferably being continuously available so that adjustment may be made in the amount of air delivered to the digestion basin in accordance with the oxygen level in the sewage. Thus, apparatus 10 is usable to permit either periodic or continuous determination of the amount of dissolved oxygen in the digestion basin of a sewage tank with it being possible to control air supply mechanism directly from the testing apparatus through suitable current sensitive devices and control units which are conventional in the electronic control field.
  • Apparatus 10 also is useful for measuring dissolved oxygen in sea water which is important in oceanographic studies related to presence and number of fishes, fish migration studies and similar purposes. Apparatus 10 also has utility for measuring dissolved oxygen in all types of saline water and any natural water streams having the four hundred parts per million dissolved solids therein. With respect to saline water, the test apparatus is particularly useful for measuring the amount of dissolved oxygen in the brine present in oil wells, to permit correction of those conditions which can cause corrosion when excess amounts of oxygen are present in the brine subjected to high heat from the drill bit.
  • apparatus 10 in measuring the amount of dissolved oxygen in a liquid is not fully understood, but it is known that the thallium electrode 44 reacts with oxygen in the liquid to produce thallous hydroxide thereby resulting in a release of electrons which flow through the conductive liquid to the lead electrode 40 thereby producing a current which is quantitatively measured by meter 14. Since the amount of oxygen reacting with the thallium electrode 44 is relatively small per unit of time, it is to be understood that even though the electrode is used up over a period of time, it does have a relatively long, useful life requiring only infrequent replacement.
  • Electrodes 40, 42 and 44 are chosen because of their relative positions in the electromotive force series with lead having an electrode potential of 0.80 while thallium has an electrode potential of +0330.
  • the electrode potential of aluminum is +1.70. It is therefore, apparent that the total potential difference between the thallium and lead electrodes i 1.13 while the potential difference ,between the aluminum electrode and thallium is 1.37.
  • the fiow of electrons will be in opposite directions from the thallium to the lead than from the aluminum to the thallium so that currents in opposite directions are created in the cell produced when the probe defined by electrodes 40, 42 and 44 is immersed in a liquid containing oxygen and dissolved solids therein.
  • Meter 14 thereby read an effective current since the two currents actually produced between the electrodes but in opposite directions result in a cancellation of the smallest current and a corresponding reduction in the intensity of the other current.
  • the addition of the aluminum electrode 42 in parallel relationship with lead electrode 4-!) with respect to meter 14, provides a bucking current to the current between the thallium and the lead which is the primary circuit of the measuring device and which tends to cancel out variations that occur because of temperature differences when diiferent readings are taken. For example, if the temperature of the solution under test increases, thereby tending to cause the meter reading to change because of decrease in the specific resistance of the solution, a greater amount of electrons are also caused to flow in an opposite direction between the aluminum and thallium electrodes and effectively cancelling out the increase of electron flow between the thallium and the lead. It appears that the cancellation current is sufiiciently linear with respect to the primary current between the thallium and the lead, to prevent distortion of the meter readings by variations in temperature of the solution under test.
  • the protective membrane 46 around each of the electrodes 40, 4-2 and 44, is also important since cellulose acetate and cellulose nitrate of the thickness employed are permeable only to inorganic ions, thereby resulting in exclusion of organic materials from the surface of the electrodes which would form corrosive and undesirable deposits thereon afiecting the accuracy of the test instrument. Furthermore, with respect to the thallium elecrode, the membrane also prevents wear corrosion which could occur because of the fiow of liquid past the probe vhile the latter is immersed in the liquid. Since thallium is a relatively soft metal, impingement of liquid thereagainst could cause the electrode to rapidly wear away and require frequent replacement thereof, but more importantly, would render the readings on meter 14 inaccurate.
  • the voltage divider 54 permits calibration of the test apparatus for accurate readings within the tolerances of the components used with the instrument preferably being precalibrated before shipping and normally not requiring any field calibration during use.
  • the apparatus 10 be used for continuous testing procedures, it is normally desirable that the same be connected to a recorder of any suitable type wit-h the lead of the recorder being connected to the terminals 26 and 28 respectively in conjunction with shifting of the operating arm of switch 22 into the Record location with the switch arms 48 and 6-8 in engagement with the contacts 82 and 85 respectively.
  • Apparatus 'for measuring the amount of dissolved oxygen in an electrically conductive liquid containing a major proportion of water comprising:
  • first conductor means connecting the thallium electrode to one of the terminals
  • second conductor means connecting the aluminum and 6 lead electrodes in parallel relationship to the other bf said terminals.
  • liquid receiving container mean adapted to removably receive the electrodes therein and in disposition with the support resting on and supported by the container means.
  • Apparatus for measuring the amount of oxygen in an electrically conductive liquid containing a major proportion of water comprising:
  • first, second and third electrodes adapted to be immersed in said liquid, said second electrode having a position in the electromotive series between the respective positions of said first and third electrodes and being of a material characterized by its tendency to vary in electromotive potential in response to a variance in the oxygen content of said liquid, there being electrical means consisting of a conductor directly interconnecting and serving as the sole conductive path between said first and third electrodes; and
  • electrically actuated current measuring mechanism coupled electrically in series with and between said second electrode and said electrical means to measure the algebraic sum of the oppositely directed galvanic currents generated between said first and second electrodes and said second and third electrodes during reaction of said second electrode with oxygen and thereby the quantity of oxygen in said liquid.
  • Apparatus for measuring the amount of dissolved oxygen in an electrically conductive liquid c'on-taining a major proportion of water comprising:
  • one of said electrodes being reactive with dissolved oxygen in the liquid and having a position in the electromotive series between the respective positions of the remaining electrodes;

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)

Description

April 11, 1967 R. H. ROBINSQN 3,333,72Q
APPARATUS FOR MEASURING DISSOLVED OXYGEN IN WATER Filed April .19, 1963 IN MENTOR. Pic-hard H02 ROM/780m United States Patent 3,313,724 APPARATUS FOR MEASURING DISSOLVED OXY EN EN WATER Richard Hoe Robinson, Kansas City, Mo., assignor to Labconco Corporation, a corporation of Missouri Filed Apr. 19, 1963, Ser. No. 274,219 9 Claims. (Cl. 204-195) This invention relates to apparatus for determining the dissolved oxygen content of a liquid and particularly to a direct reading instrument capable of indicating the amount of dissolved oxygen in the liquid by the simple expedient of the operator immersing a probe in the liquid and visually observing the reading on a dissolved oxygen indicator.
The amount of dissolved oxygen in a liquid such as water, has heretofore been a relatively difiicult analytical operation because of the small amount of oxygen which is actually present in the water and the complicated tests which must be performed in order to accurately determine the presence and amount of the oxygen which is dissolved in the liquid. In most instances, the amount of dissolved oxygen in the liquid will not exceed about ten parts per million and, therefore, requiring very sensitive instruments operated by relatively skilled technicians. Furthermore, it has not heretofore been possible to maintain an accurate surveillance on the amount of dissolved oxygen in a body of water and permitting utilization of the analytical instrument as a device for varying the amount of air or oxygen which is supplied to the water to maintain the dissolved oxygen at a predetermined level.
It is, therefore, the primary object of the present invention to provide apparatus for measuring dissolved oxygen in a liquid such as water, which requires no laboratory procedures, provides an immediate visual indication of the amount of oxygen in a body of liquid, and which is completely portable for use at any desired location without outside current sources or accessory instruments.
It is another important object of the invention to provide apparatus for measuring dissolved oxygen in Water employing probe structure which maybe immersed in the liquid and having measuring means operably connected thereto for giving a visual indication of the amount of oxygen in the liquid, whereby all chemical tests and gas analysis test operations previously required, are completely obviated.
A particularly important object of the invention is to provide apparatus as described above, which is utilizable under varying conditions and with the dissolved oxygen readings being accurate within reasonable tolerances, regardless of normal temperature variations in the liquid being measured and the rate of flow thereof relative to the test apparatus,
A still further important aim of the invention is to provide apparatus for measuring dissolved oxygen in water wherein the probe is made up of electrodes of thallium, lead and aluminum respectively, operably coupled to a current measuring device so that the amount of oxygen in a liquid in which the probe is immersed, may be readily determined by virtue of reaction of the thallium with the oxygen, thereby producing a measurable current between the electrodes. In this respect, another significant object of the invention is to provide apparatus as referred to :above, wherein the aluminum electrode is connected to one terminal of the current measuring device, while the thallium and lead electrodes are connected in parallel relationship to the other terminal so that currents of opposite direction are produced between the electrodes to thereby provide compensation for temperature variations in the liquid being tested.
Patented Apr. H, 1957 Another very important object of the invention is to provide apparatus employing an electrode probe of thallium, lead and aluminum electrodes operably coupled to a measuring device wherein an ion permeable membrane is provided around each of the electrodes to prevent variations in the flow rates of the liquid being tested atfecting the readings of the current measuring device.
Another object of the invention is to provide apparatus capable of measuring the dissolved oxygen content in a flowing liquid which is particularly useful for determining the amount of oxygen in sewage within a sewage treatment facility 50 that the apparatus may be coupled through servo-mechanism or the like to structure for delivering controlled amounts of air or oxygen to the body of sewage in response to variations in the oxygen content sensed by the test apparatus.
In the drawing:
FIG. 1 is an elevational view of portable test apparatus for measuring the amount of dissolved oxygen in a liquid and constructed in accordance with the preferred Concepts of the present invention, with the probe and container thereof being shown to one side of the instrument case for clarity of illustration;
FIG. 2 is a plan view of the apparatus illustrated in FIG. 1 and showing the probe and container therefor in normal disposition on the rear face of the instrument case;
FIG. 3 is a schematic representation of the probe and operating circuit therefor provided within the test instrument case; and
FIG. 4 is a greatly enlarged horizontal cross-sectional view taken substantially on line 4-4 of FIG. 1.
Apparatus capable of measuring dissolved oxygen in water, in accordance with the present invention, is broadly designated It in the drawing, and includes a generally rectangular instrument case 12 mounting a visually observable microammeter 14 on the front face panel 16 thereof so that the operator may readily observe the location of needle 18 with reference to the linear scale 2t). The front face panel 16 of case 12 also mounts a double pole double throw toggle switch 22, a selectively adjustable potentiometer control 24, and a pair of terminals 26 and 28 identified with appropriate positive and negative indicia on panel 16.
A generally U-shaped clip 3% secured to the rear surface 32 of case 12 and projecting outwardly therefrom, is adapted to removably receive a general cylindrical, open top container 34 of transparent, synthetic resin material and adapted to receive a quantity of liquid 36 therein, such as water. The upper opening defining extremity of container 34 is internally threaded to complementally receive the external threads of a mounting block 38 which serves as means for mounting elongated, generally cylindrical electrodes 40, 42 and 44 respectively.
Electrode 40 is preferably of lead, electrode 42 of aluminum and electrode 44 of thallium.
The upper extremities of the electrodes, as illustrated in FIG. 3, are embedded in block 38 in disposition with the longitudinal axes thereof being in generally parallel relationship with the outer surfaces of the same in equidistant relationship and thereby located at the apices of an imaginary equilateral triangle. The electrodes are also of substantially equal length, as is apparent from FIGS. 1 and 3. A membrane 46 of an ion permeable material is provided around each of the electrodes 40, 42 and 44 in completely encasing relationship thereto with the membrane preferably being of cellulose acetate or cellulose nitrate. In any event, the membrane should be of propperties and thickness permitting inorganic ions to pass therethrough but precluding passage of organic molecules and other particles of similar size or larger therethrough.
The thallium electrode 44 is connected to the switch arm 48 of selector switch 22 by line while the coil 52 of potentiometer 54 is interposed in a line 56 leading from lead electrode 40 to line 5-0. Line 53 serves to join aluminum electrode 42 directly to line 56. The movable contact 69 of potentiometer 54 is coupled to the positive terminal 62 of microammeter 14 by line 64 while the negative terminal 66 of microarnmeter 14 is joined to switch arm 63 of selector switch 22 by line 74}.
A load resistor 72 is provided in line 74 between contacts 76 and 78 of switch 22 while line 86 connects terminal 26 to contact 82 of switch 22 and line 84 couples contact 86 of switch 22 to terminal 28. As noted schematically in FIG. 3, switch arms 43 and 68 are suitably ganged.
The conductor lines 56 and 58 extending from case 12 to mounting block 33, are suitably encased in an insulating sheath 83 which is of sufficient length to be immersed in a liquid at a substantial distance from case 12. Thus, suitable brackets 90 are provided on surface 32 of case 12 in outwardly extending relationship therefrom, serving as means for storing sheath 88 and the conductors therein when wound around the brackets, as illustrated in FIG. 2. Handle 92 on the top of case 12 facilitates manual transportation of apparatus 10.
In operation, the container 34 is removed from mounting block 38 and the probe, defined by electrodes 40, 42 and 44 is immersed in the liquid to be tested for dissolved oxygen content. The toggle switch 22 is placed in disposition normally designated as Indicate whereby the switch arms 48 and 68 will be in the disposition thereof illustrated in FIG. 3, placing the load resistor 72 in circuit with the ammeter 14. If the liquid to be measured comprises a flowing stream, it is only necessary that the probe be held in the liquid so that a direct reading may be observed on the dial of meter 14. However, if the water is still, since some water movement or flow is required for accurate determination of the amount of oxygen in the liquid, the probe should be moved back and forth while reading the disposition of needle 18 with respect to the indicia of scale 2t).
It has been determined that the liquid containing dissolved oxygen must have approximately four hundred parts per million of dissolved solids in the liquid .in order to give a correct reading on meter 14. Dissolved solids in the context used herein means primarily those materials which will ionize and thus includes inorganic salts although certain types of organic materials would also fall into this catergory. However, if the liquid to be tested does in fact have four hundred parts per million or more of dissolved solids therein, it has been determined that the reading of needle 18 on scale 20 gives a direct indication of the amount of oxygen in the liquid being tested. Empirical studies have shown that the amount of current measured by meter 14 is linearly related to the amount of oxygen in the liquid.
Since apparatus is especially useful for measuring dissolved oxygen in water that contains at least four hundred parts per million of dissolved solids, it has been determined that the most important utility of the present structure is concerned with measurement of the amount of oxygen in sewage within the digestion basin of a sewage treatment facility. It is well known that the amount of oxygen present in the digestion basin of a sewage treatment plant is an extremely important parameter that must be maintained at a predetermined value or above in order to obtain most efficient treatment of the raw sewage. For this reason, it is desirable to have an accurate method available of determining the :amount of oxygen in the sewage in the digestion basin and with such information preferably being continuously available so that adjustment may be made in the amount of air delivered to the digestion basin in accordance with the oxygen level in the sewage. Thus, apparatus 10 is usable to permit either periodic or continuous determination of the amount of dissolved oxygen in the digestion basin of a sewage tank with it being possible to control air supply mechanism directly from the testing apparatus through suitable current sensitive devices and control units which are conventional in the electronic control field.
Apparatus 10 also is useful for measuring dissolved oxygen in sea water which is important in oceanographic studies related to presence and number of fishes, fish migration studies and similar purposes. Apparatus 10 also has utility for measuring dissolved oxygen in all types of saline water and any natural water streams having the four hundred parts per million dissolved solids therein. With respect to saline water, the test apparatus is particularly useful for measuring the amount of dissolved oxygen in the brine present in oil wells, to permit correction of those conditions which can cause corrosion when excess amounts of oxygen are present in the brine subjected to high heat from the drill bit.
The exact operation of apparatus 10 in measuring the amount of dissolved oxygen in a liquid is not fully understood, but it is known that the thallium electrode 44 reacts with oxygen in the liquid to produce thallous hydroxide thereby resulting in a release of electrons which flow through the conductive liquid to the lead electrode 40 thereby producing a current which is quantitatively measured by meter 14. Since the amount of oxygen reacting with the thallium electrode 44 is relatively small per unit of time, it is to be understood that even though the electrode is used up over a period of time, it does have a relatively long, useful life requiring only infrequent replacement.
Electrodes 40, 42 and 44 are chosen because of their relative positions in the electromotive force series with lead having an electrode potential of 0.80 while thallium has an electrode potential of +0330. The electrode potential of aluminum is +1.70. It is therefore, apparent that the total potential difference between the thallium and lead electrodes i 1.13 while the potential difference ,between the aluminum electrode and thallium is 1.37. However, the fiow of electrons will be in opposite directions from the thallium to the lead than from the aluminum to the thallium so that currents in opposite directions are created in the cell produced when the probe defined by electrodes 40, 42 and 44 is immersed in a liquid containing oxygen and dissolved solids therein. Meter 14 thereby read an effective current since the two currents actually produced between the electrodes but in opposite directions result in a cancellation of the smallest current and a corresponding reduction in the intensity of the other current.
The utilization of aluminum electrode 42 which pro duces a bucking current to that introduced between elec= trodes 40 and 44, has been found to provide compensation for temperature differentials encountered during dissolved oxygen measurements so that within practical limits, an accurate reading can be obtained on the scale 20 of meter 14 without regard to the temperature of the solution being tested. Thus, direct readings are obtained without compensating formulas being needed or complicated components within apparatus 10 for automatically providing temperature compensation. It is recognized that the degree of ionization in a 'liquid containing ionizable materials, is dependent upon the temperature of the solution a well as the concentration of the ionizable materials therein. Thus, upon increase in temperature of the solution a higher degree of ionization is obtained, thereby affecting the amount of current that may flow through the solution, thus altering the reading which would be obtained on meter 14 if only lead and thallium electrodes were employed for the probe. Since the specific resistance of a solution varies with the degree of ionization of the electrolyte therein, variation of the degree of ionization of the materials in the solution between the electrodes will also cause a variation on the reading of the meter as the specific resistance changes with temperature differentials. For this reason, upon in crease in temperature of the solution under test, even though the dissolved oxygen content would remain the same in the solution, the meter reading would change because of lowering of the specific resistance of the solution. By the same token, lowering of the temperature of the test solution would have the opposite effect and the meter reading would be less even though the dissolved oxygen content remained constant.
It is believed that the addition of the aluminum electrode 42 in parallel relationship with lead electrode 4-!) with respect to meter 14, provides a bucking current to the current between the thallium and the lead which is the primary circuit of the measuring device and which tends to cancel out variations that occur because of temperature differences when diiferent readings are taken. For example, if the temperature of the solution under test increases, thereby tending to cause the meter reading to change because of decrease in the specific resistance of the solution, a greater amount of electrons are also caused to flow in an opposite direction between the aluminum and thallium electrodes and effectively cancelling out the increase of electron flow between the thallium and the lead. It appears that the cancellation current is sufiiciently linear with respect to the primary current between the thallium and the lead, to prevent distortion of the meter readings by variations in temperature of the solution under test.
As above noted, it is necessary that the liquid under test be flowing past the electrodes of the probe during the test so that oxygen in the solution is always available to react with the thallium in order to give an accurate indication on scale 29. Thus, if the liquid is not flowing, the same result can be obtained by moving the probe back and forth while observing the reading 'on scale 29.
The protective membrane 46 around each of the electrodes 40, 4-2 and 44, is also important since cellulose acetate and cellulose nitrate of the thickness employed are permeable only to inorganic ions, thereby resulting in exclusion of organic materials from the surface of the electrodes which would form corrosive and undesirable deposits thereon afiecting the accuracy of the test instrument. Furthermore, with respect to the thallium elecrode, the membrane also prevents wear corrosion which could occur because of the fiow of liquid past the probe vhile the latter is immersed in the liquid. Since thallium is a relatively soft metal, impingement of liquid thereagainst could cause the electrode to rapidly wear away and require frequent replacement thereof, but more importantly, would render the readings on meter 14 inaccurate.
The voltage divider 54 permits calibration of the test apparatus for accurate readings within the tolerances of the components used with the instrument preferably being precalibrated before shipping and normally not requiring any field calibration during use. When it is desired that the apparatus 10 be used for continuous testing procedures, it is normally desirable that the same be connected to a recorder of any suitable type wit-h the lead of the recorder being connected to the terminals 26 and 28 respectively in conjunction with shifting of the operating arm of switch 22 into the Record location with the switch arms 48 and 6-8 in engagement with the contacts 82 and 85 respectively.
Having thus described the invention what is claimed as new and desired to be secured by Letters Patent is:
1. Apparatus 'for measuring the amount of dissolved oxygen in an electrically conductive liquid containing a major proportion of water, said apparatus comprising:
three elongated electrodes of thallium, lead and aluminum respectively, and adapted to be immersed in said liquid;
an amrneter having a pair of terminals;
first conductor means connecting the thallium electrode to one of the terminals; and
second conductor means connecting the aluminum and 6 lead electrodes in parallel relationship to the other bf said terminals.
2. Apparatus as set forth in claim 1, wherein said electrodes are mounted on a common support therefor and located in equidistantly spaced, generally parallel relationship.
3. Apparatus as set forth in claim 2, wherein is provided open top, liquid receiving container mean adapted to removably receive the electrodes therein and in disposition with the support resting on and supported by the container means.
4. Apparatus for measuring the amount of oxygen in an electrically conductive liquid containing a major proportion of water, said apparatus comprising:
first, second and third electrodes adapted to be immersed in said liquid, said second electrode having a position in the electromotive series between the respective positions of said first and third electrodes and being of a material characterized by its tendency to vary in electromotive potential in response to a variance in the oxygen content of said liquid, there being electrical means consisting of a conductor directly interconnecting and serving as the sole conductive path between said first and third electrodes; and
electrically actuated current measuring mechanism coupled electrically in series with and between said second electrode and said electrical means to measure the algebraic sum of the oppositely directed galvanic currents generated between said first and second electrodes and said second and third electrodes during reaction of said second electrode with oxygen and thereby the quantity of oxygen in said liquid.
5. Apparatus for measuring the amount of dissolved oxygen in an electrically conductive liquid c'on-taining a major proportion of water, said apparatus comprising:
three electrode adapted to be immersed in said liquid,
one of said electrodes being reactive with dissolved oxygen in the liquid and having a position in the electromotive series between the respective positions of the remaining electrodes;
electrical means consisting of a conductor directly interconnecting and serving as the sole conductive path between said remaining electrodes; and
means electrically connected in series with and between said electrical means and said one electrode for measuring the galvanic current therebetween generated during reaction of oxygen with said one electrode whereby the amount of current measured is a function of the dissolved oxygen content of the liquid and whereby the current between one of said remaining electrodes and said one electrode opposes and at least partially cancels the current between said one electrode and the other of said remaining electrodes to thereby provide compensation for temperature variations of the liquid.
6. Apparatus as set forth in claim 5, wherein said one electrode is of thallium.
7. Apparatus as set forth in claim 5, wherein said one of said remaining electrodes is of lead.
8. Apparatus a set forth in claim 5, wherein said other of said remaining electrodes is of aluminum.
9. Apparatus as set forth in claim 5, wherein said electrodes are located in equidistant relationship at the apices of an imaginary triangle defined thereby.
References Cited by the Examiner UNITED STATES PATENTS 2,288,180 6/1942 Brengman et al 204-495 2,510,262 6/1950 Sollner et a1. 204 2,805,191 9/1957 Hersch 2041 2,912,367 11/1959 Asendorf et al. 204195 (Other references on following page) UNITED '7 STATES PATENTS Beard 204-495 Carnitt et a1 204-195 Jessop 204-195 Cohn et a1 204-195 Juda. Digby 204195 Capuano 204-195 8 4/ 1966 Allsopp 204-195 5/1966 Seyl 204-195 OTHER REFERENCES Le Baron at 211.: Trans. of the Electrochemical Soc, Volume LXXVII, 1940, pages 289-297.
JOHN H. MACK, Plilfllll")? Examiner.
T. H. TUNG, Assistant Examiner.

Claims (1)

  1. 4. APPARATUS FOR MEASURING THE AMOUNT OF OXYGEN IN AN ELECTRICALLY CONDUCTIVE LIQUID CONTAINING A MAJOR PROPORTION OF WATER, SAID APPARATUS COMPRISING: FIRST, SECOND AND THIRD ELECTRODES ADAPTED TO BE IMMERSED IN SAID LIQUID, SAID SECOND ELECTRODE HAVING A POSITION IN THE ELECTROMOTIVE SERIES BETWEEN THE RESPECTIVE POSITINS OF SAID FIRST AND THIRD ELECTRODES AND BEING OF A MATERIAL CHARACTERIZED BY ITS TENDENCY TO VARY IN ELECTROMOTIVE POTENTIAL IN RESPONSE TO A VARIANCE IN THE OXYGEN CONTENT OF SAID LIQUID, THERE BEING ELECTRICAL MEANS CONSISTINGOF A CONDUTOR DIRECTLY INTERCONNECTING AND SERVING AS THE SOLE CONDUCTIVE PATH BETWEEN SAID FIRST AND THIRD ELECTRODES; AND ELECTRICALLY ACTUATED CURRENT MEASURING MECHANISM COUPLED ELECTRICALLY IN SERIES WITH AND BETWEEN SAID SECOND ELECTRODE AND SAID ELECTRICAL MEANS TO MEASURE THE ALGEBRAIC SUM OF THE OPPOSITELY DIRECTED GALVANIC CURRENTS GENERATED BETWEEN SAID FRIST AND SECOND ELECTRODES AND SAID SECOND AND THIRD ELECTRODES DURING REACTION OF SAID SECOND ELECTRODE WIT OXYGEN AND THEREBY THE QUANTITY OF OXYGEN IN SAID LIQUID.
US274219A 1963-04-19 1963-04-19 Apparatus for measuring dissolved oxygen in water Expired - Lifetime US3313720A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US274219A US3313720A (en) 1963-04-19 1963-04-19 Apparatus for measuring dissolved oxygen in water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US274219A US3313720A (en) 1963-04-19 1963-04-19 Apparatus for measuring dissolved oxygen in water

Publications (1)

Publication Number Publication Date
US3313720A true US3313720A (en) 1967-04-11

Family

ID=23047299

Family Applications (1)

Application Number Title Priority Date Filing Date
US274219A Expired - Lifetime US3313720A (en) 1963-04-19 1963-04-19 Apparatus for measuring dissolved oxygen in water

Country Status (1)

Country Link
US (1) US3313720A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3437524A (en) * 1966-10-05 1969-04-08 Us Air Force Solid electrolyte alkali metal voltaic cell
US3455807A (en) * 1964-08-03 1969-07-15 Mine Safety Appliances Co Gas detector
US3513079A (en) * 1965-01-06 1970-05-19 Nat Res Dev Method and apparatus for measuring the concentration of dissolved gas in a liquid
US4042465A (en) * 1976-08-25 1977-08-16 Lexington Instrument Corporation Measurement of oxygen in a fluid sample and apparatus therefor
US5527444A (en) * 1994-04-19 1996-06-18 Sweeney, Jr.; John W. Probe having coaxial design for use with dissolved oxygen meter
US5690808A (en) * 1996-01-25 1997-11-25 Teledyne Industries, Inc. Electrochemical gas sensors and methods for sensing electrochemical active gases in gas mixtures
US5763762A (en) * 1992-01-13 1998-06-09 Sweeney, Jr.; John W. Total dissolved gas pressure sensor, replaceable collector module and process
US7664607B2 (en) 2005-10-04 2010-02-16 Teledyne Technologies Incorporated Pre-calibrated gas sensor

Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2288180A (en) * 1938-06-08 1942-06-30 Beatrice Creamery Company Apparatus for measuring ph
US2510262A (en) * 1944-09-08 1950-06-06 Univ Minnesota Process of making ionic membranes
US2805191A (en) * 1952-01-16 1957-09-03 Int Nickel Co Oxygen analysis of gases
US2912367A (en) * 1957-04-26 1959-11-10 Degussa Measurement of cyanide concentration
US2927888A (en) * 1956-02-08 1960-03-08 Honeywell Regulator Co Measuring apparatus
US3000805A (en) * 1957-08-30 1961-09-19 Walter G Finch Electrode measuring device
US3022241A (en) * 1957-02-15 1962-02-20 Cambridge Instr Company Inc Method and apparatus for measurement of dissolved oxygen
US3080444A (en) * 1960-06-28 1963-03-05 Engelhard Ind Inc Electric cell
US3124520A (en) * 1959-09-28 1964-03-10 Electrode
US3196100A (en) * 1961-09-07 1965-07-20 Cambridge Instr Company Inc Oxygen detecting and measuring apparatus
US3218242A (en) * 1962-01-04 1965-11-16 Union Carbide Corp Measurement of the concentration of dissolved oxygen in liquids
US3246235A (en) * 1960-12-30 1966-04-12 Atomic Energy Authority Uk Apparatus for oxygen analysis of gases
US3250689A (en) * 1965-05-03 1966-05-10 Robert G Seyl Simplified method of measuring corrosion using reference electrode

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2288180A (en) * 1938-06-08 1942-06-30 Beatrice Creamery Company Apparatus for measuring ph
US2510262A (en) * 1944-09-08 1950-06-06 Univ Minnesota Process of making ionic membranes
US2805191A (en) * 1952-01-16 1957-09-03 Int Nickel Co Oxygen analysis of gases
US2927888A (en) * 1956-02-08 1960-03-08 Honeywell Regulator Co Measuring apparatus
US3022241A (en) * 1957-02-15 1962-02-20 Cambridge Instr Company Inc Method and apparatus for measurement of dissolved oxygen
US2912367A (en) * 1957-04-26 1959-11-10 Degussa Measurement of cyanide concentration
US3000805A (en) * 1957-08-30 1961-09-19 Walter G Finch Electrode measuring device
US3124520A (en) * 1959-09-28 1964-03-10 Electrode
US3080444A (en) * 1960-06-28 1963-03-05 Engelhard Ind Inc Electric cell
US3246235A (en) * 1960-12-30 1966-04-12 Atomic Energy Authority Uk Apparatus for oxygen analysis of gases
US3196100A (en) * 1961-09-07 1965-07-20 Cambridge Instr Company Inc Oxygen detecting and measuring apparatus
US3218242A (en) * 1962-01-04 1965-11-16 Union Carbide Corp Measurement of the concentration of dissolved oxygen in liquids
US3250689A (en) * 1965-05-03 1966-05-10 Robert G Seyl Simplified method of measuring corrosion using reference electrode

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3455807A (en) * 1964-08-03 1969-07-15 Mine Safety Appliances Co Gas detector
US3513079A (en) * 1965-01-06 1970-05-19 Nat Res Dev Method and apparatus for measuring the concentration of dissolved gas in a liquid
US3437524A (en) * 1966-10-05 1969-04-08 Us Air Force Solid electrolyte alkali metal voltaic cell
US4042465A (en) * 1976-08-25 1977-08-16 Lexington Instrument Corporation Measurement of oxygen in a fluid sample and apparatus therefor
US5763762A (en) * 1992-01-13 1998-06-09 Sweeney, Jr.; John W. Total dissolved gas pressure sensor, replaceable collector module and process
US5527444A (en) * 1994-04-19 1996-06-18 Sweeney, Jr.; John W. Probe having coaxial design for use with dissolved oxygen meter
US5690808A (en) * 1996-01-25 1997-11-25 Teledyne Industries, Inc. Electrochemical gas sensors and methods for sensing electrochemical active gases in gas mixtures
US7664607B2 (en) 2005-10-04 2010-02-16 Teledyne Technologies Incorporated Pre-calibrated gas sensor

Similar Documents

Publication Publication Date Title
US2947679A (en) Corrosion rate sensing assembly
US2913386A (en) Electrochemical device for chemical analysis
US3406101A (en) Method and apparatus for determining corrosion rate
US2830945A (en) Apparatus for water determination
US3924175A (en) D.C. system for conductivity measurements
US2531747A (en) Metal identifier
Pearson “Null” Methods Applied to Corrosion Measurements
US4056445A (en) Determination of corrosion rates by an electrochemical method
US3313720A (en) Apparatus for measuring dissolved oxygen in water
US3331021A (en) A. c. corrosion-rate meter and method
Burrows et al. The Li/Li+ reference electrode in propylene carbonate
US2949765A (en) Measuring circuit for fluid analyzers
US3022241A (en) Method and apparatus for measurement of dissolved oxygen
Briggs et al. Use of the wide-bore dropping-mercury electrode for long-period recording of concentration of dissolved oxygen
US3061773A (en) Apparatus for cathodic protection
US3338812A (en) Electrolytic titration apparatus
US3305457A (en) Hydrocarbon detection
GB913490A (en) Apparatus for measuring corrosion
Neville Electrochemical device for measuring oxygen
US3069332A (en) Simplification in method of measuring corrision of electronic conductors by non-gaseous ionic conductors
US3662256A (en) Hydroxyl ion measuring system
Lorimer et al. Optical and electrical methods of determining transference numbers of electrolytes in dilute solutions by the moving boundary technique
Merritt et al. Apparatus for Automatic Controlled Potential Electrolysis Using Electronic Coulometer
Palmer et al. Thermal-conductivity method for the analysis of gases
US3398065A (en) Method and apparatus for measuring corrosion rate